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Researchers found that certain RNA circles in the brain are linked to disease risk, but their exact role in disease is still unknown.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

Hair loss gene found on chromosome 3q26.

A specific gene variation in goats is linked to better growth traits.

Certain genetic variants impair enzyme activity, contributing to non-classic congenital adrenal hyperplasia.

Human and horse hair have similar end groups to wool and feathers.

Modified β-catenin causes different effects in hair and skin cells, leading to cysts or tumors.

NCSTN gene mutation causes abnormal skin cell differentiation and more inflammation, contributing to Hidradenitis Suppurativa.

Cantu syndrome, which causes excessive hair growth and skin issues, is due to a mutation in the ABCC9 gene, and understanding this could help develop new treatments for hair diseases.

A specific gene mutation causes woolly hair and hair loss.

Cyclic ADP-ribose helps regulate calcium and signals that promote hair growth in hair follicle cells.

Beta-catenin boosts hair follicle cell growth by increasing c-myc expression.

A gene called Taqpep affects cat coat patterns like stripes and blotches.

Robertsonian translocation can cause recurrent miscarriages.

The Eda gene helps regulate the hair cycle in goats.

The FGF5 gene variant causes long hair in Akitas, and genetic testing is advised to manage coat length and welfare.

A specific gene mutation causes sparse, brittle hair in a family.

Variants on chromosome 10 affect hair thickness in Dazu black goats.

Some human genetic markers work for genetic studies in pig-tailed and stump-tailed macaques, which can help in their conservation.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

CaBP1 and 2 are necessary for maintaining calcium currents and hearing in inner ear cells.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

KAP8.2 gene variations affect cashmere quality in goats.

Key circRNAs play a role in wool follicle development, aiding in breeding better quality wool sheep.

Some canine hair follicle tumors contain amyloid deposits, with a protein called CK5 involved in their formation.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

A specific gene variant may increase the risk of developing Alopecia Areata.

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A new genetic mutation in the CAST gene may link PLACK syndrome to alopecia areata.